WHOLE GENOME SEQUENCING
The complete
picture of
your health.
Most DNA tests read 0.02% of your genome. We analyze all of it.
Get the complete clinical picture you need to anticipate health risks, target treatments, and address complex symptoms.
FIND YOUR SITUATION
Who We Help
HEREDITARY RISK
It runs in your family. Now you can know if it runs in your genes.
Your genome contains inherited variants associated with cardiac, cancer, and neurological conditions. We read all of them.
UNEXPLAINED SYMPTOMS
When traditional lab tests say you're fine. And you know you're not.
Standard diagnostics check for a pre-selected set of answers. We sequence your full DNA, including parts no test was designed to check.
TREATMENT NOT WORKING
Your diagnosis may be right. Your treatment plan may be incomplete.
Your genes determine which treatments work and which do not. We give your doctor the pharmacogenomic data to inform the plan.
PROACTIVE HEALTH
You want to know before something forces the question.
Your genome reveals predispositions years before symptoms appear. Acting on that knowledge is the definition of preventive medicine.
ALREADY TESTED
You already took a DNA test. Here's what it couldn't tell you.
Most consumer DNA tests read a fraction of your genome. We read all of it and deliver clinically actionable reports your doctor can use.
THE CLINICAL ADVANTAGE
Standard genetic tests miss 99.98% of your DNA.
Diagnostic Depth
We sequence every base pair of your genome at 30X clinical coverage. Not a panel. Not an array. The complete genetic picture, read with the precision required for diagnostic decisions.
Unrestricted Discovery
Targeted tests only find what they're designed to look for. WGS reads your entire genome, including intergenic regions, structural variants, and areas of the genome that panels simply skip.
Permanent Relevance
Your DNA doesn't change, but science is accelerating. Every month, new variant-disease associations are discovered. We validate these findings and update your reports automatically, for life.
COVERAGE COMPARISON
100%
Dante Whole Genome Sequencing
Every gene. Every region. Every base pair. 30X clinical-grade coverage across your entire genome.
~0.1%
Targeted Gene Panels
Limited to a pre-selected set of genes. Misses structural variants, intergenic regions, and the vast majority of your genome.
<0.02%
Microarray Tests
Checks only known SNPs. Cannot detect novel variants, structural changes, or anything outside predefined positions.
CLINICAL COVERAGE
What We Find
Your genome holds answers across every area of medicine. Here are the categories our 200+ reports cover.
CARDIAC
Inherited cardiac conditions
Cardiomyopathies, arrhythmias, aortopathies, and familial hypercholesterolemia. Variants that affect heart structure and function, often asymptomatic until a critical event.
ONCOLOGY
Hereditary cancer predisposition
BRCA1/2, Lynch syndrome, Li-Fraumeni, and dozens of other hereditary cancer syndromes. Knowing your risk profile enables earlier screening and targeted prevention.
NEUROLOGICAL
Neurological and neurodegenerative
Variants associated with Alzheimer's, Parkinson's, epilepsy, and hereditary neuropathies. Early identification supports proactive management and clinical planning.
RARE DISEASE
Rare and undiagnosed conditions
Over 7,000 rare diseases have a genetic basis. WGS is the only test capable of screening for all of them in a single analysis, ending diagnostic odysseys that can last years.
PHARMACOGENOMICS
Drug response and metabolism
Your genes affect how you metabolize medications. Pharmacogenomic data helps your physician select the right drug at the right dose, reducing adverse reactions and improving efficacy.
UNEXPLAINED SYMPTOMS
Complex and unexplained cases
When symptoms don't fit a known pattern, the answer may sit in parts of the genome that standard tests never examine. WGS provides the complete dataset for clinical investigation.
"They never added the numbers up until now when they saw the Dante Labs report. That result changed everything."
Thomas, Scotland
Queen Elizabeth University Hospital Glasgow, NHS
30X
whole genome coverage
5M
variants identified
200+
clinical reports
99.98%
sequencing accuracy
Thomas spent years with a set of symptoms no specialist had been able to connect into a coherent picture. Despite dozens of consultations and traditional tests, his condition remained a mystery.
It wasn't until he received his Dante Labs Whole Genome report that the underlying genetic cause was finally identified. By reading his entire DNA, our analysis connected the disparate clinical markers that had previously gone unnoticed.
Sometimes the genome finds something your doctors weren't looking for.
INCLUDED IN YOUR TEST
What You Receive
30X Clinical Sequencing
Your entire genome sequenced at 30X coverage in a CLIA-certified, CAP-accredited laboratory. The same standard used for clinical diagnostic decisions.
200+ Physician-Ready Reports
Organized by clinical category. Easy to read, designed for you and your doctor to act on. Not raw data files, actionable health reports.
100% Raw Data Ownership
Your genome belongs to you. Download your complete raw data (FASTQ, BAM, VCF) at any time. Use it with any compatible analysis tool or share with your clinician.
Secure Genome Manager
All reports delivered through your personal Genome Manager portal. Encrypted, HIPAA-compliant, and accessible from any device. Reports update automatically as science advances.
CLINICAL INFRASTRUCTURE
Clinical Standards
CAP / CLIA Accredited
Our laboratory holds dual accreditation from the College of American Pathologists (CAP) and Clinical Laboratory Improvement Amendments (CLIA). The highest standard for clinical laboratory operations in the United States.
ISO 15189 Certified
International accreditation for medical laboratories, covering both technical competence and quality management systems. Recognized in over 80 countries for diagnostic-grade results.
ACMG Guidelines
All variant classifications follow the American College of Medical Genetics and Genomics guidelines. Pathogenic, likely pathogenic, VUS, and benign classifications aligned with current clinical consensus.
GET STARTED
One test. A lifetime of discovery.
One kit, sent to your home. Your entire genome sequenced at the clinical standard used for diagnostic decisions. 200+ physician-ready reports delivered to your Genome Manager in 6 to 8 weeks. Permanent and updated as science advances.
FROM
$449
Ships within 48 hours · Results in 6 to 8 weeks
BNPL / HSA / FSA ELIGIBLE